Canonical Allele Identifier: CA4451143

Gene: CFTR

Linked Data

• ClinVar Variation Id: 1429889
• ClinVar RCV Id: RCV001967369 ; RCV002479476
• dbSNP Id: rs745538406
• ExAC: 7:117232334 A / G
• gnomAD v2: 7-117232334-A-G
• gnomAD v4: 7-117592280-A-G
• MyVariant Identifiers: chr7:g.117232334A>G (hg19) ; chr7:g.117592280A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117592280A>G , CM000669.2:g.117592280A>G	GRCh38
NC_000007.13:g.117232334A>G , CM000669.1:g.117232334A>G	GRCh37
NC_000007.12:g.117019570A>G	NCBI36
NG_016465.4:g.131497A>G , LRG_663:g.131497A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.2113A>G	ENSP00000497673.2:p.Ile705Val
ENST00000647978.2:c.*1827A>G	ENSP00000497658.1:n.*1827A>G
ENST00000649781.2:c.1930A>G	ENSP00000497203.1:p.Ile644Val
ENST00000685018.2:c.2113A>G	ENSP00000510194.2:p.Ile705Val
ENST00000687278.2:c.2113A>G	ENSP00000509593.2:p.Ile705Val
ENST00000699585.1:c.2113A>G	ENSP00000514456.1:p.Ile705Val
ENST00000699598.1:c.2113A>G	ENSP00000514467.1:p.Ile705Val
ENST00000699599.1:c.2113A>G	ENSP00000514468.1:p.Ile705Val
ENST00000699600.1:c.2113A>G	ENSP00000514469.1:p.Ile705Val
ENST00000699601.1:c.*413A>G	ENSP00000514470.1:n.*413A>G
ENST00000699602.1:c.2113A>G	ENSP00000514471.1:p.Ile705Val
ENST00000699604.1:c.*1937A>G	ENSP00000514472.1:n.*1937A>G
ENST00000699605.1:c.1687A>G	ENSP00000514473.1:p.Ile563Val
ENST00000003084.11:c.2113A>G MANE Select	ENSP00000003084.6:p.Ile705Val
ENST00000647978.1:c.*1827A>G	ENSP00000497658.1:n.*1827A>G
ENST00000648260.1:c.1402-10546A>G	ENSP00000497957.1:n.1402-10546A>G
ENST00000649406.1:c.1930A>G	ENSP00000497965.1:p.Ile644Val
ENST00000649781.1:c.1930A>G	ENSP00000497203.1:p.Ile644Val
ENST00000003084.10:c.2113A>G	ENSP00000003084.6:p.Ile705Val
ENST00000426809.5:c.2023A>G	ENSP00000389119.1:p.Ile675Val
NM_000492.3:c.2113A>G , LRG_663t1:c.2113A>G	NP_000483.3:p.Ile705Val
XM_011515751.1:c.2203A>G	XP_011514053.1:p.Ile735Val
XM_011515752.1:c.2203A>G	XP_011514054.1:p.Ile735Val
XM_011515753.1:c.1870A>G	XP_011514055.1:p.Ile624Val
XM_011515754.1:c.1870A>G	XP_011514056.1:p.Ile624Val
NM_000492.4:c.2113A>G MANE Select	NP_000483.3:p.Ile705Val